BASF Drug For Further Processing
NDC Database

BASF Drug For Further Processing

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Drug for Further Processing
  • Total Records 2
  • Latest Marketing Date 2019-03-31
  • Data Source FDA
  • First Marketing Date 2005-01-14
All
24
View
Bulk Ingredient
22
View
Drug for Further Processing
2
View
Company Overview

Company

BASF Drug For Further Processing

Country

Germany

Website

Visit Website

Email

global.info@basf.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

BASF Drug For Further Processing

Carl-Bosch-Strasse 38 Ludwigshafen , Rhineland-Palatinate 67056

Germany

pharmaceutical.basf.com/global/en.html global.info@basf.com View on Map
NDC Records ( 2 records )
2019
31 Mar
Drug for Further Processing NDC: 10117-3009

Nonproprietary Name

ZINC OXIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

BASF Corporation

Marketing Category

DRUG FOR FURTHER PROCESSING

10117-3009

Substance

ZINC OXIDE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2019-03-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
14 Jan
Drug for Further Processing NDC: 10117-3613

Nonproprietary Name

Octinoxate, Avobenzone

Dosage Form

LIQUID

Strength

1; 1 kg/kg; kg/kg

Labeler

BASF Corporation

Marketing Category

DRUG FOR FURTHER PROCESSING

10117-3613

Substance

AVOBENZONE; OCTINOXATE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2005-01-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
2 total
  • Drug for Further Processing
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

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NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

10117-3009

Nonproprietary Name

ZINC OXIDE

Labeler

BASF Corporation

Dosage Form

POWDER

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NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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